Characterization and heterologous reconstitution of Taxus biosynthetic enzymes leading to baccatin III

Science. 2024 Feb 9;383(6683):622-629. doi: 10.1126/science.adj3484. Epub 2024 Jan 25.

Abstract

Paclitaxel is a well known anticancer compound. Its biosynthesis involves the formation of a highly functionalized diterpenoid core skeleton (baccatin III) and the subsequent assembly of a phenylisoserinoyl side chain. Despite intensive investigation for half a century, the complete biosynthetic pathway of baccatin III remains unknown. In this work, we identified a bifunctional cytochrome P450 enzyme [taxane oxetanase 1 (TOT1)] in Taxus mairei that catalyzes an oxidative rearrangement in paclitaxel oxetane formation, which represents a previously unknown enzyme mechanism for oxetane ring formation. We created a screening strategy based on the taxusin biosynthesis pathway and uncovered the enzyme responsible for the taxane oxidation of the C9 position (T9αH1). Finally, we artificially reconstituted a biosynthetic pathway for the production of baccatin III in tobacco.

MeSH terms

  • Alkaloids* / biosynthesis
  • Alkaloids* / genetics
  • Bridged-Ring Compounds / chemistry
  • Bridged-Ring Compounds / metabolism
  • Cytochrome P-450 Enzyme System* / chemistry
  • Cytochrome P-450 Enzyme System* / genetics
  • Ethers, Cyclic / chemistry
  • Ethers, Cyclic / metabolism
  • Metabolic Engineering*
  • Paclitaxel* / biosynthesis
  • Plant Proteins* / chemistry
  • Plant Proteins* / genetics
  • Taxoids* / metabolism
  • Taxus* / enzymology
  • Taxus* / genetics

Substances

  • Alkaloids
  • baccatin III
  • Bridged-Ring Compounds
  • Ethers, Cyclic
  • oxetane
  • Paclitaxel
  • taxane
  • Taxoids
  • Cytochrome P-450 Enzyme System
  • Plant Proteins